A. Konstantinidou is granted by REA Maternity Clinic, grant nr 70/3/11191.
Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: Novel association with pectus carinatum in a molecularly confirmed case and review of the fetal phenotype
Article first published online: 29 NOV 2013
Copyright © 2013 Wiley Periodicals, Inc.
Birth Defects Research Part A: Clinical and Molecular Teratology
Volume 97, Issue 12, pages 774–780, December 2013
How to Cite
Konstantinidou, A. E., Tasoulas, J., Kallipolitis, G., Gasparatos, S., Velissariou, V. and Paraskevakou, H. (2013), Mandibulofacial dysostosis (Treacher-Collins syndrome) in the fetus: Novel association with pectus carinatum in a molecularly confirmed case and review of the fetal phenotype. Birth Defects Research Part A: Clinical and Molecular Teratology, 97: 774–780. doi: 10.1002/bdra.23202
- Issue published online: 17 DEC 2013
- Article first published online: 29 NOV 2013
- Manuscript Accepted: 27 SEP 2013
- Manuscript Revised: 11 SEP 2013
- Manuscript Received: 16 JUL 2013
- Treacher Collins syndrome;
- Pierre Robin sequence;
- cleft palate;
- pectus carinatum;
Treacher Collins syndrome is the most common mandibulofacial dysostosis of autosomal dominant or, rarely, recessive inheritance. Affected fetuses may be identified by prenatal ultrasound or diagnosed at autopsy in case of perinatal death or pregnancy termination.
We describe the ultrasonographic, autopsy, and molecular findings in a 25-week-gestation affected fetus, and review the clinical, prenatal, and postmortem findings in 15 previously reported fetal and perinatal cases.
A nearly complete spectrum of the typical facial characteristics can be present by the early second trimester of gestation, including subtle defects such as lower eyelid colobomas. Mandibular hypoplasia and bilateral auricle defects were constant findings in the affected fetal population. Downslanting palpebral fissures were the second more common feature, followed by midface hypoplasia, polyhydramnios, and ocular defects. Association with Pierre Robin sequence was common (38%) in the reviewed series. Previously unreported pectus carinatum was noted in our case bearing a heterozygous TCOF1 mutation. Other unique reported findings include salivary gland hyperplasia, single umbilical artery, and tracheo-esophageal fistula, all in molecularly unconfirmed cases.
Treacher Collins syndrome can be prenatally detected by ultrasound and should be included in the wide range of genetic syndromes that can be diagnosed at perinatal autopsy. Affected fetuses tend to have a more severe phenotype than living patients. The reported association of Treacher Collins syndrome type 1 with pectus carinatum expands the phenotype, provides information on genotype–phenotype correlation, and suggests possible pathogenetic interactions between neural crest cell disorders and the formation of the sternum that merit investigation. Birth Defects Research (Part A), 97:774–780, 2013. © 2013 Wiley Periodicals, Inc.